ENST00000475243.6:c.194C>T
MANE Select
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ENSP00000417175.1:p.Ala65Val
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ENST00000265619.6:n.492C>T
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|
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ENST00000395802.7:c.194C>T
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ENSP00000379147.3:p.Ala65Val
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ENST00000475243.5:c.194C>T
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ENSP00000417175.1:p.Ala65Val
|
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ENST00000520497.1:c.194C>T
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ENSP00000430426.1:p.Ala65Val
|
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NM_001195677.1:c.194C>T
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NP_001182606.1:p.Ala65Val
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NM_004738.4:c.194C>T , LRG_656t1:c.194C>T
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NP_004729.1:p.Ala65Val
|
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NR_036633.1:n.535C>T
|
|
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XR_001754433.2:n.443C>T
|
|
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NM_001195677.2:c.194C>T
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NP_001182606.1:p.Ala65Val
|
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NM_004738.5:c.194C>T
MANE Select
|
NP_004729.1:p.Ala65Val
|
|
NR_036633.2:n.425C>T
|
|
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